Mutation analysis of phenylketonuria in Spain: prevalence of two Mediterranean mutations

Hum Genet. 1992 May;89(3):341-2. doi: 10.1007/BF00220555.

Abstract

We have screened seven Spanish phenylketonuric (PKU) families for the most prevalent Mediterranean and Caucasian mutations, and have subsequently found mutations P281L and IVS10. We have analyzed these two mutations in 23 of our patients. The frequencies found correspond to those of Mediterranean countries, such as Italy. This is the first report of a mutation analysis in the Spanish PKU population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Frequency / genetics
  • Humans
  • Mutation / genetics
  • Phenylalanine Hydroxylase / deficiency
  • Phenylalanine Hydroxylase / genetics*
  • Phenylketonurias / epidemiology
  • Phenylketonurias / genetics*
  • Polymerase Chain Reaction
  • Spain / epidemiology
  • White People / genetics

Substances

  • Phenylalanine Hydroxylase